34 results match your criteria: "St Anna Hospital and University[Affiliation]"

isomiRs, the sequence-variants of microRNA, are known to be tissue and cell type specific but their physiological role is largely unknown. In our study, we explored for the first time the expression of isomiRs across different Stage I epithelial ovarian cancer (EOC) histological subtypes, in order to shed new light on their biological role in tumor growth and progression. In a multicentric retrospective cohort of tumor biopsies (n = 215) we sequenced small RNAs finding 971 expressed miRNAs, 64% of which are isomiRs.

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Background: Stage I epithelial ovarian cancer (EOC) encompasses five histologically different subtypes of tumors confined to the ovaries with a generally favorable prognosis. Despite the intrinsic heterogeneity, all stage I EOCs are treated with complete resection and adjuvant therapy in most of the cases. Owing to the lack of robust prognostic markers, this often leads to overtreatment.

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Hidradenitis suppurativa (HS), together with other inflammatory diseases, is involved in a syndromic network where different combinations of signs and symptoms characterize the definition. The observation of the concurrent occurrence of HS, pyoderma gangrenosum (PG), and inflammatory bowel disease (IBD), in detail ulcerative colitis (UC), led the authors to describe a new association. The patient, a 36-year-old woman, who saw IBD as the first appearing condition, shortly followed by HS and PG, was referred because of a clinical situation quickly worsening.

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Orbital Fractures in Childhood.

Ann Maxillofac Surg

January 2019

Department of Cranio-Maxillofacial Surgery, Unit of Cranio-Maxillofacial Surgery, St. Anna Hospital and University, Ferrara, Italy.

Pediatric orbital floor fractures exhibit distinctive features that distinguish them from orbital injuries seen in the adult population. This is mainly due to different anatomy and mechanical properties of the orbital bones in children. The management of pediatric orbital floor fractures requires consideration of these factors, including the age of the patient and therefore child's growth potential, using, if possible, a minimally invasive surgical approach.

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Novel design of miniplate for fixation of fractures at transition zone of parasymphysis-body region of mandible - A clinical randomised study.

J Craniomaxillofac Surg

October 2019

EACMF Education and Training Officer, Unit of CranioMaxilloFacial Surgery, St. Anna Hospital and University, Viale Aldo Moro, 8, Ferrara, 44124, Cona, Italy. Electronic address:

Fractures through the mandible at the level of the parasymphysis extending obliquely and traversing through the transitional zone to body region are relatively common. Therefore, a surgeon should have an appropriate understanding of the biomechanics of different plating techniques to fix these fractures. There is always a dilemma for the surgeon as to whether to fix these mandibular segments with one or two miniplates, and the presence of mental neurovascular bundle makes it more challenging.

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Posttraumatic Glabellar Mucocele: Case Report.

Craniomaxillofac Trauma Reconstr

December 2018

Unit of Craniomaxillofacial Surgery, St. Anna Hospital and University, Ferrara, Italy.

Mucoceles are benign, expansile cystic masses covered by respiratory epithelium filled with mucus secreted by goblet cells interspersed in the ciliated mucosa. Mucoceles result from the accumulation and retention of the products of secretion, desquamation, and inflammation in cases where the drainage is obstructed. We present a case of a nasal mucocele that developed in a 50-year-old man, possibly related to a craniofacial trauma that had occurred 24 years earlier.

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The mandibular parasymphysis and body regions are highly dynamic areas. They are constantly subjected to both occlusal and muscular forces. Fractures at this transition zone of the parasymphysis and body region thus represent a special pattern that creates a dilemma for the surgeons - whether to use one miniplate fixation or two miniplates as per Champy's guidelines.

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Craniomaxillofacial Fibrous Dysplasia: Conservative Treatment and Maxillary Osteotomy Using the Schuchardt-Kufner Technique.

Craniomaxillofac Trauma Reconstr

March 2018

Unit of Cranio-Maxillo-Facial Surgery, Centre for Orbital Pathology and Surgery, Reference Center for Treatment of Rare Disease, St. Anna Hospital and University, Ferrara, Italy.

Fibrous dysplasia (FD) is a disturbance of the mesenchymal tissue that accounts for 2.5% of all bone tumors and more than 7% of nonmalignant bone tumors. In the craniomaxillofacial region, FD affects the calvaria, skull base, zygoma, and jaws, the prevalent site being the maxilla (50% of cases).

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Temporomandibular Joint Ankylosis After Early Mandibular Distraction Osteogenesis: A New Syndrome?

J Craniofac Surg

July 2017

Unit of Cranio Maxillo Facial Surgery, Reference Center for Rare Craniofacial Anomalies, European Association for Cranio Maxillofacial Surgery, International Teaching Center Network, St. Anna Hospital and University, Ferrara, Italy.

Distraction osteogenesis (DO) has been one of the most innovative concepts in cranio-maxillofacial syndromology and surgery over the last 25 years.Early mandibular distraction in severe micrognathia has recently been recognized as an effective treatment option to safely relieve upper airway obstruction associated with mandibular deficiency.An increased incidence in temporomandibular joint complications during DO in neonates has recently been reported, especially in syndromic patients.

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Silent Sinus Syndrome is defined as a painless spontaneous and progressive enophthalmos and hypoglobus with maxillary sinus hypoplasia and orbital floor resorption. It is caused by maxillary sinus atelectasis in a setting of ipsilateral chronic maxillary sinus hypoventilation. The syndrome was first described in 1964 by Montgomery, but the term "Silent Sinus Syndrome" was not coined until 1994 by Soparkar.

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The Buccal Fat Pad for Closure of Oroantral Communication.

J Craniofac Surg

May 2016

Unit of Cranio Maxillo Facial Surgery, Reference Center for Cranio-Facial Rare Anomalies European Association for Cranio Maxillofacial Surgery, International Teaching Center Network, St. Anna Hospital and University, Ferrara, Italy.

The buccal fat pad (BFP) is a well-established tool in oral and maxillofacial surgery and its use has proved of value for the closure of oroantral communications. Oroantral communication may be a common complication after sequestrectomy in "bisphosphonate-related osteonecrosis of the jaws."The authors report a clinical case of a 70-year-old female patient in bisphosphonate therapy presented with right maxillary sinusitis and oroantral communication after implants insertion.

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Treatment of exophthalmos and strabismus surgery in thyroid-associated orbitopathy.

Int J Oral Maxillofac Surg

June 2016

Unit of Cranio-Orbito-Maxillofacial Surgery, St. Anna Hospital and University, Ferrara, Cona, Italy.

Endocrine orbitopathy (EO) can have important consequences, such as exophthalmos and restrictive strabismus. A retrospective study was performed of 35 patients with EO who underwent orbital decompression surgery and restrictive strabismus correction. Two surgical techniques for orbital decompression were analyzed: fat decompression by Olivari technique and three-wall bony expansion with fat decompression.

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Piezosurgery: A new and safe technique for distraction osteogenesis in Pierre Robin sequence review of the literature and case report.

Int J Surg Case Rep

January 2015

Unit of Cranio Maxillo Facial Surgery, Center for Orbital Pathology & Surgery, Reference Center for Treatment of Rare Diseases, EACMFS International Teaching Centers Network, St. Anna Hospital and University, Via Aldo Moro n. 8 Cona (FE), Ferrara 44124, Italy.

Introduction: Pierre Robin sequence (PRS) is characterized by microgenia and retrognathia. Cleft palate and glossoptosis are frequently associated with airway obstruction and difficulty in swallowing. Distraction osteogenesis with micro-distractors has recently been considered as a surgical option during the neonatal age.

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Unexpected death from cardiac involvement in acute granulomatosis with polyangiitis (Wegener's): clinical and histopathologic features.

J Cardiovasc Med (Hagerstown)

January 2015

aDepartment of Nephrology and Dialysis bDepartment of Surgery, St. Andrea Hospital, La Spezia cDepartment of Forensic Medicine, University of Pavia, Pavia dDepartment of Pathological Anatomy eDepartment of Cardiology, Spedali Civili and University of Brescia, Brescia fDepartment of Internal Medicine, St. Anna Hospital and University of Ferrara, Ferrara gDepartment of Nephrology and Dialysis, Spedali Civili and University of Brescia, Brescia, Italy.

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Cranial bone grafts in forehead reconstruction after resection for benign tumors.

J Craniofac Surg

March 2013

Unit of Cranio Maxillo Facial Surgery, Center for Craniofacial Deformities & Orbital Surgery, St Anna Hospital and University, Ferrara, Italy.

Cranial bone graft was first used in forehead reconstruction by Muller and König as early as 1890. Because cranial bone graft is the ideal material for almost all facial and skull repairs, surgeons have subsequently used this technique to repair skull defects. In fact, membranous bone (calvaria) is superior to endochondral bone (ilium, rib) and maintains its volume to a significantly greater extent than endochondral bone.

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Craniofacial surgical strategies for the correction of pneumosinus dilatans frontalis.

J Craniomaxillofac Surg

January 2013

Unit of Cranio Maxillo Facial Surgery, Center for Orbital Pathology & Surgery, St. Anna Hospital and University, Ferrara, Italy.

Introduction: Pneumosinus dilatans is a rare condition and different techniques have been proposed for its management and correction. The abnormally expanded, aerated frontal sinus has been described in the literature as: frontal sinus hypertrophy, pneumosinus dilatans, pneumosinus frontalis, aerocele, pneumocele, sinus ectasia, hyperpneumatization and others. The precise aetiology and pathogenesis of the condition is unknown, although several basic hypotheses have been proposed

Material And Methods: The authors report two cases of frontal bossing and supraorbital ridge deformity correction using craniofacial surgical principles.

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Frontal linear scleroderma: long-term result in volumetric restoration of the fronto-orbital area by structural fat grafting.

J Craniofac Surg

May 2012

Unit of Cranio Maxillo Facial Surgery, Center for Craniofacial Deformities & Orbital Surgery, St Anna Hospital and University, Ferrara, Italy.

Frontal linear scleroderma (also known as "en coup de sabre") is a congenital deformity characterized by a linear band of atrophy and a furrow in the skin that occurs in the frontal or frontoparietal area. The authors present a case of a 34-year-old woman with history of en coup de sabre. In different steps, volumetric restoration of the fronto-orbital region has been obtained by structural fat grafting technique.

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Contouring of the forehead irregularities (washboard effect) with bone biomaterial.

J Craniofac Surg

May 2012

Unit of Cranio Maxillo Facial Surgery, Center for Craniofacial Deformities & Orbital Surgery, St Anna Hospital and University, Ferrara, Italy.

Calvarial vault defects may be repaired with autologous bone or alloplastic materials, such as methyl methacrylate, hydroxyapatite, titanium, or porous polyethylene. The criterion standard for repairing small cranial defects is autogenous bone from iliac crest or split calvarial grafts. However, autogenous grafts may result in donor-site morbidity, increased operative time, reabsorption, blood loss, and additional time for recovery.

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Pigmented villonodular synovitis is a benign lesion of unclear etiology involving the synovial membranes of joints, bursae, and tendon sheaths. Its occurrence in the temporomandibular joint is particularly rare. Despite its benign nature, pigmented villonodular synovitis is described as being locally destructive to the surrounding structures.

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Endocrine orbitopathy (EO) represents the most frequent and important extrathyroidal stigma of Graves disease. This chronic autoimmune condition involves the orbital contents, including extraocular muscles, periorbital connective-fatty tissue and lacrimal gland. The increase of fat tissue and the enlargement of extraocular muscles within the bony confines of the orbit leads to proptosis, and in the most severe cases optic neuropathy, caused by compression and stretching of the optic nerve.

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Endocrine orbitopathy: 11 years retrospective study and review of 102 patients & 196 orbits.

J Craniomaxillofac Surg

February 2012

Unit of Cranio Maxillo Facial Surgery, Center for Craniofacial Deformities & Orbital Surgery, St. Anna Hospital and University, Corso Giovecca 203, 44100 Ferrara, Italy.

Background: Endocrine Orbitopathy (EO) is the most frequent and important extrathyroidal stigma of Graves' disease. In the active stage of the orbitopathy fibrosis and hypertrophy of the extra-ocular muscles can lead to visual impairment and diplopia. In the stable phase of the disease surgical treatment by orbital expansion and/or orbital decompression can improve the quality of life and it is indicated for morpho-aesthetic and functional reasons.

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Structural fat grafting: facial volumetric restoration in complex reconstructive surgery.

J Craniofac Surg

September 2011

Unit of Cranio Maxillo Facial Surgery, Center for Craniofacial Deformities & Orbital Surgery, St Anna Hospital and University, Corso Giovecca, 203, 44100 Ferrara, Italy.

Background: The authors overview the application of structural fat grafting (SFG) in the management of volumetric deficit in the maxillofacial area. Structural fat grafting was introduced as a way to improve facial aesthetics and in recent years has evolved into applications in craniomaxillofacial reconstructive surgery.

Methods: A retrospective cohort study population was composed of patients grafted with autologous fat referred to our department from February 2005 to July 2009.

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Peripheral ameloblastoma: case report.

Minerva Stomatol

September 2011

Center for Craniofacial Deformities and Orbital Surgery, St. Anna Hospital and University, Ferrara, Italy.

Ameloblastoma is a benign tumour of the odontogenic tissues which may be aggressive in the involved area with a high rate of recurrence if not adequately removed, and represents 1% of all tumours of the mouth, generally appearing in the bones of the jaw. Although it is fairly rare, tumours with such histopathology have been described in the soft tissue and are named peripheral or extraosseus ameloblastoma. Potential cells of origin are ondontogenic residue of the dental lamina, pluripotent cells in the basal layer of the epithelial mucosa, and pluripotent cells of the minor salivary glands.

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Endocrine orbitopathy (Graves disease): transpalpebral fat decompression in combination with 3-wall bony expansion.

J Craniofac Surg

July 2010

Unit of Cranio Maxillo Facial Surgery, Centre for Craniofacial Deformities and Orbital Surgery, and Department of Ophthalmology, St Anna Hospital and University, 44100 Ferrara, Italy.

Endocrine orbitopathy (EO) is a chronic, multisystem autoimmune disorder caused by lymphocyte infiltration, edema, and proliferation of endo-orbital connective tissue. These conditions involve the extraocular muscles, intraconal and extraconal fat, and, to a lesser extent, the lacrimal gland.Endocrine orbitopathy may be associated with toxic diffuse goiter and/or pretibial myxedema (Graves disease) and may appear without alterations in thyroid function (euthyroidism).

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